Structural and biochemical characterization of the Clostridium perfringens autolysin catalytic domain

FEBS Lett. 2017 Jan;591(1):231-239. doi: 10.1002/1873-3468.12515. Epub 2016 Dec 19.

Abstract

Bacterial autolysins can partially hydrolyze cell wall peptidoglycans into small sections to regulate cell separation/division and the growth phase. Clostridium perfringens autolysin (Acp) has an N-terminal cell wall-binding domain and a C-terminal catalytic domain with glucosaminidase activity that belongs to the glycoside hydrolase 73 family. Here, we determined the X-ray structure of the Acp catalytic domain (AcpCD) at 1.76 Å resolution. AcpCD has a unique crescent-shaped structure, forming a deep groove for substrate-binding at the center of the protein. The modeling study of the enzyme/substrate complex demonstrated that the length of the substrate-binding groove is closely related to the glucosaminidase activity. Mutagenesis analysis showed that AcpCD likely adopts a neighboring-group mechanism for the catalytic reaction.

Keywords: X-ray structure; autolysin; glycoside hydrolase 73 family.

Publication types

  • Letter

MeSH terms

  • Amino Acid Sequence
  • Bacteriolysis
  • Catalytic Domain*
  • Clostridium perfringens / enzymology*
  • Crystallography, X-Ray
  • Models, Molecular
  • Mutagenesis / genetics
  • N-Acetylmuramoyl-L-alanine Amidase / chemistry*
  • N-Acetylmuramoyl-L-alanine Amidase / metabolism*
  • Peptidoglycan / chemistry
  • Peptidoglycan / metabolism
  • Substrate Specificity

Substances

  • Peptidoglycan
  • N-Acetylmuramoyl-L-alanine Amidase

Associated data

  • PDB/3FI7
  • PDB/5AZM
  • PDB/2XEN
  • PDB/5WQW